Pub Date : 2021-07-04DOI: 10.1080/02603594.2021.1922396
M. Khatami, S. Iravani
ABSTRACT Two-dimensional MXenes with their attractive applicability and unique properties such as eco-friendly features, large surface area, remarkable chemical stability, high thermal/electrical conductivity, exclusive sorption-reduction capacity, and hydrophilicity can be employed as promising candidates for water treatment; they can be mostly deployed for the elimination of various hazardous pollutants with high sorption selectivity, efficient reduction capability, and suitable degradation potentials. However, several important physicochemical parameters (e.g., pH, temperature, and water quality) can influence the adsorption performance of MXenes. Additionally some important challenging issues regarding the toxicity, degradability, storage, and large scale/commercial production of MXenes are still need to be evaluated. The aggregation of MXenes is also a critical challenge, which can reduce the adsorption activity and surface area of these materials; the surface chemistry of MXenes and related mechanisms of contaminants removal by these materials should be analytically and systematically evaluated. Importantly, the environmental risks of MXene-based structures should also be broadly analyzed. This review delineates the pros and cons and critical issues pertaining to the deployment of MXenes endowed with their superior surface area, high selectivity/sensitivity, recyclability, and attractive mechanical properties for removing hazardous pollutants (e.g., antibiotics, dyes, pesticides, heavy metals, pharmaceutical compounds, and radionuclides) from water and wastewater. GRAPHICAL ABSTRACT
{"title":"MXenes and MXene-based Materials for the Removal of Water Pollutants: Challenges and Opportunities","authors":"M. Khatami, S. Iravani","doi":"10.1080/02603594.2021.1922396","DOIUrl":"https://doi.org/10.1080/02603594.2021.1922396","url":null,"abstract":"ABSTRACT Two-dimensional MXenes with their attractive applicability and unique properties such as eco-friendly features, large surface area, remarkable chemical stability, high thermal/electrical conductivity, exclusive sorption-reduction capacity, and hydrophilicity can be employed as promising candidates for water treatment; they can be mostly deployed for the elimination of various hazardous pollutants with high sorption selectivity, efficient reduction capability, and suitable degradation potentials. However, several important physicochemical parameters (e.g., pH, temperature, and water quality) can influence the adsorption performance of MXenes. Additionally some important challenging issues regarding the toxicity, degradability, storage, and large scale/commercial production of MXenes are still need to be evaluated. The aggregation of MXenes is also a critical challenge, which can reduce the adsorption activity and surface area of these materials; the surface chemistry of MXenes and related mechanisms of contaminants removal by these materials should be analytically and systematically evaluated. Importantly, the environmental risks of MXene-based structures should also be broadly analyzed. This review delineates the pros and cons and critical issues pertaining to the deployment of MXenes endowed with their superior surface area, high selectivity/sensitivity, recyclability, and attractive mechanical properties for removing hazardous pollutants (e.g., antibiotics, dyes, pesticides, heavy metals, pharmaceutical compounds, and radionuclides) from water and wastewater. GRAPHICAL ABSTRACT","PeriodicalId":10481,"journal":{"name":"Comments on Inorganic Chemistry","volume":"19 1","pages":"213 - 248"},"PeriodicalIF":5.4,"publicationDate":"2021-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87727311","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-06-20DOI: 10.1080/02603594.2021.1938007
P. Bagus, C. Nelin, C. Brundle, B. Crist, N. Lahiri, K. Rosso
ABSTRACT XPS analyses of open shell ionic compounds, especially oxides of the first row transition metals, for information such as oxidation state tend to focus on characteristics of the metal 2p XPS features alone. These analyses could be made considerably more robust with simultaneous characterization of the XPS of the metal 3p features as well as the 2p features. In these comments, we provide a perspective on the conceptual and theoretical framework needed to extract chemical information from the complex multiplet structure of the 3p XPS of Fe oxides as representative of 3d transition metal oxides. We also present information about a novel kind of many-body effects that may contribute to a further redistribution of the Fe 3p XPS intensity. The concern here is not to develop a complicated mathematical formalism but to explain the complexity in terms of fundamental quantum mechanical concepts. This is done on the basis of ab initio Dirac Hartree–Fock wavefunctions where we examine the physical nature of the 3p XPS features of the representative ferrous and ferric oxides of FeO and Fe2O3, respectively. The key objectives of this paper are as follows: (1) to demonstrate the importance of the angular momentum coupling of open shell electrons, which is done more easily with RS multiplets; (2) to show that a single configuration description of the final state multiplets is woefully inadequate; (3) to identify a novel atomic many-body effect that can lead to a rich satellite structure. The considerations discussed here should have implications for making useful interpretations of the XPS of lower BE levels of other ionic, high spin materials. This paper provides a manifestation of a new tradition by which Comments on Inorganic Chemistry starts publishing original research content that, nonetheless, preserves the Journal’s identity as a niche for critical discussion of contemporary literature in inorganic chemistry; for previous manifestations, see Comments Inorg. Chem. 2020, 40, 277–303 and references cited in the abstract thereof.
{"title":"Comments on the Theory of Complex XPS Spectra: Extracting Chemical Information from the Fe 3p XPS of Fe Oxides","authors":"P. Bagus, C. Nelin, C. Brundle, B. Crist, N. Lahiri, K. Rosso","doi":"10.1080/02603594.2021.1938007","DOIUrl":"https://doi.org/10.1080/02603594.2021.1938007","url":null,"abstract":"ABSTRACT XPS analyses of open shell ionic compounds, especially oxides of the first row transition metals, for information such as oxidation state tend to focus on characteristics of the metal 2p XPS features alone. These analyses could be made considerably more robust with simultaneous characterization of the XPS of the metal 3p features as well as the 2p features. In these comments, we provide a perspective on the conceptual and theoretical framework needed to extract chemical information from the complex multiplet structure of the 3p XPS of Fe oxides as representative of 3d transition metal oxides. We also present information about a novel kind of many-body effects that may contribute to a further redistribution of the Fe 3p XPS intensity. The concern here is not to develop a complicated mathematical formalism but to explain the complexity in terms of fundamental quantum mechanical concepts. This is done on the basis of ab initio Dirac Hartree–Fock wavefunctions where we examine the physical nature of the 3p XPS features of the representative ferrous and ferric oxides of FeO and Fe2O3, respectively. The key objectives of this paper are as follows: (1) to demonstrate the importance of the angular momentum coupling of open shell electrons, which is done more easily with RS multiplets; (2) to show that a single configuration description of the final state multiplets is woefully inadequate; (3) to identify a novel atomic many-body effect that can lead to a rich satellite structure. The considerations discussed here should have implications for making useful interpretations of the XPS of lower BE levels of other ionic, high spin materials. This paper provides a manifestation of a new tradition by which Comments on Inorganic Chemistry starts publishing original research content that, nonetheless, preserves the Journal’s identity as a niche for critical discussion of contemporary literature in inorganic chemistry; for previous manifestations, see Comments Inorg. Chem. 2020, 40, 277–303 and references cited in the abstract thereof.","PeriodicalId":10481,"journal":{"name":"Comments on Inorganic Chemistry","volume":"24 1","pages":"373 - 397"},"PeriodicalIF":5.4,"publicationDate":"2021-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78823957","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-06-11DOI: 10.1080/02603594.2021.1922395
H. Bhasin, Divya R. Mishra
ABSTRACT With the emerging and alarming environmental deterioration and weakening of human health have become a global menace which have posed severe potential impact on the worldwide growing concern for the ecological conditions. Metal Organic Frameworks, a class of porous, robust and rigid compounds has been effectively fascinated and categorized for their versatile role as luminescent detectors and adsorbents for harmful anthropogenic pollutants from the environment . In this review, we aim to update the database of several MOFs which emphasize the role of MOFs, and their mechanism based on the luminescent detection and adsorptive removal of different anthropogenic pollutants. Moreover, we have tried a plausible way to relate these two applications to adapt the design, synthesis and experimental strategies of MOFs for simultaneous detection and adsorptive removal of anthropogenic contaminants.
{"title":"Metal Organic Frameworks: A Versatile Class of Hybrid Compounds for Luminescent Detection and Adsorptive Removal of Enviromental Hazards","authors":"H. Bhasin, Divya R. Mishra","doi":"10.1080/02603594.2021.1922395","DOIUrl":"https://doi.org/10.1080/02603594.2021.1922395","url":null,"abstract":"ABSTRACT With the emerging and alarming environmental deterioration and weakening of human health have become a global menace which have posed severe potential impact on the worldwide growing concern for the ecological conditions. Metal Organic Frameworks, a class of porous, robust and rigid compounds has been effectively fascinated and categorized for their versatile role as luminescent detectors and adsorbents for harmful anthropogenic pollutants from the environment . In this review, we aim to update the database of several MOFs which emphasize the role of MOFs, and their mechanism based on the luminescent detection and adsorptive removal of different anthropogenic pollutants. Moreover, we have tried a plausible way to relate these two applications to adapt the design, synthesis and experimental strategies of MOFs for simultaneous detection and adsorptive removal of anthropogenic contaminants.","PeriodicalId":10481,"journal":{"name":"Comments on Inorganic Chemistry","volume":"4 1","pages":"267 - 315"},"PeriodicalIF":5.4,"publicationDate":"2021-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73296757","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-04-11DOI: 10.1080/02603594.2021.1904912
Nasrin Shafiei, M. Nasrollahzadeh, S. Iravani
ABSTRACT Silica and silicon nanomaterials have diverse applications in the field of drug/gene delivery, lightweight aggregates, regenerative medicine, tissue engineering, cancer diagnosis/therapy, catalytic applications, and energy storage. There is an increasing demand for eco-friendly synthesis of silica and silicon nanomaterials with enough cost-effectiveness, safety, reliability, simplicity, scalability, and controllable particle size distribution features. These materials can be effectively obtained from various agrarian sustainable bio-resources, including rice husk ash, sugar-cane, coffee husk, wheat husk and corn cob ash. Using green and sustainable techniques can cause to eliminate or reduce laborious/complicated procedures and reduce the environmental contaminants to obtain advanced materials for high-tech applications. In this review, recent advancements pertaining to the catalytic and biomedical applications of silica and silicon nanoparticles are highlighted, as well as their greener synthetic methods. Graphical Abstract
{"title":"Green Synthesis of Silica and Silicon Nanoparticles and Their Biomedical and Catalytic Applications","authors":"Nasrin Shafiei, M. Nasrollahzadeh, S. Iravani","doi":"10.1080/02603594.2021.1904912","DOIUrl":"https://doi.org/10.1080/02603594.2021.1904912","url":null,"abstract":"ABSTRACT Silica and silicon nanomaterials have diverse applications in the field of drug/gene delivery, lightweight aggregates, regenerative medicine, tissue engineering, cancer diagnosis/therapy, catalytic applications, and energy storage. There is an increasing demand for eco-friendly synthesis of silica and silicon nanomaterials with enough cost-effectiveness, safety, reliability, simplicity, scalability, and controllable particle size distribution features. These materials can be effectively obtained from various agrarian sustainable bio-resources, including rice husk ash, sugar-cane, coffee husk, wheat husk and corn cob ash. Using green and sustainable techniques can cause to eliminate or reduce laborious/complicated procedures and reduce the environmental contaminants to obtain advanced materials for high-tech applications. In this review, recent advancements pertaining to the catalytic and biomedical applications of silica and silicon nanoparticles are highlighted, as well as their greener synthetic methods. Graphical Abstract","PeriodicalId":10481,"journal":{"name":"Comments on Inorganic Chemistry","volume":"294 1","pages":"317 - 372"},"PeriodicalIF":5.4,"publicationDate":"2021-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86446520","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-04-05DOI: 10.1080/02603594.2021.1888724
Gavin Von Willingh
ABSTRACT Symmetric and asymmetric dihydroxylation reactions catalyzed by osmium have emerged as the most efficient route in the one-step synthesis of diols. This is because on an industrial scale 1,2-diols are prepared via a two-step procedure. Still, it is a challenge to prepare and apply osmium catalysts in dihydroxylation catalysis because of their safety and environmental implications; e.g., volatile, highly toxic, product contamination, etc. To date, few efforts were reported to comprehensively overcome these drawbacks with great success by heterogenizing to an insoluble matrix, including diminishment in catalytic performance. Hence, the need for efficacious solid-supported osmium catalysts to subdue these difficulties is a topic of great importance. This mini review provides a concise overview of some of the most encouraging solid-supported osmium catalysts reported over the last few years, which proved to be more efficient under mild conditions as opposed to other immobilized osmium catalytic systems. The summary discusses the latest developments in the synthetic heterogenizing and homogenization strategies, structure analysis and investigation toward symmetric and asymmetric dihydroxylation for diol production. Specific emphasis is focused on their mechanistic considerations, their reusability and improvement in their safety, and environmental implications. Graphical Abstract
{"title":"Recent Advancements in the Development of Osmium Catalysts for Various Oxidation Reactions: A New Era?","authors":"Gavin Von Willingh","doi":"10.1080/02603594.2021.1888724","DOIUrl":"https://doi.org/10.1080/02603594.2021.1888724","url":null,"abstract":"ABSTRACT Symmetric and asymmetric dihydroxylation reactions catalyzed by osmium have emerged as the most efficient route in the one-step synthesis of diols. This is because on an industrial scale 1,2-diols are prepared via a two-step procedure. Still, it is a challenge to prepare and apply osmium catalysts in dihydroxylation catalysis because of their safety and environmental implications; e.g., volatile, highly toxic, product contamination, etc. To date, few efforts were reported to comprehensively overcome these drawbacks with great success by heterogenizing to an insoluble matrix, including diminishment in catalytic performance. Hence, the need for efficacious solid-supported osmium catalysts to subdue these difficulties is a topic of great importance. This mini review provides a concise overview of some of the most encouraging solid-supported osmium catalysts reported over the last few years, which proved to be more efficient under mild conditions as opposed to other immobilized osmium catalytic systems. The summary discusses the latest developments in the synthetic heterogenizing and homogenization strategies, structure analysis and investigation toward symmetric and asymmetric dihydroxylation for diol production. Specific emphasis is focused on their mechanistic considerations, their reusability and improvement in their safety, and environmental implications. Graphical Abstract","PeriodicalId":10481,"journal":{"name":"Comments on Inorganic Chemistry","volume":"72 1","pages":"249 - 266"},"PeriodicalIF":5.4,"publicationDate":"2021-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84049223","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-03-13DOI: 10.1080/02603594.2021.1895127
M. Khatami, S. Iravani
ABSTRACT Nanophotocatalysts have numerous applications in the field of water splitting, dissociation of volatile organic pollutants, organic synthesis, degradation of dyes/hazardous contaminants, cancer cells inactivation, self-cleaning surfaces, hydrogen evolution, photo-electrochemical conversion, etc. Typically, to produce nanophotocatalysts, diverse conventional physicochemical strategies have been reported with some important drawbacks/limitations such as the utilization of toxic/hazardous materials, complex/expensive instruments, and time-consuming reactions. Therefore, there is a high demand for developing green, environmentally friendly, and cost-effective synthetic tactics, which can reduce or eliminate the rigorousness and complications of the conventional approaches. These nanophotocatalysts have shown high stability, good recyclability, and remarkable catalytic activity. Typically, the significant specific surface areas, the abundant functional groups, large amounts of active sites are the important advantages of the nanoscaled structures for highly photocatalytic degradation of organic pollutants. However, more elaborative studies are still needed to overcome some important limitations/drawbacks of nanophotocatalysts for industrial applications, which include the difficult separation, low selectivity, aggregation/sedimentation, low-usage of visible light, fast charge recombination, and low migration potential of photo-generated electrons and holes. This review highlights recent advances related to the greener and eco-friendly synthesis of nanophotocatalysts, as well as their environmental photocatalytic applications. Graphical Abstract
{"title":"Green and Eco-Friendly Synthesis of Nanophotocatalysts: An Overview","authors":"M. Khatami, S. Iravani","doi":"10.1080/02603594.2021.1895127","DOIUrl":"https://doi.org/10.1080/02603594.2021.1895127","url":null,"abstract":"ABSTRACT Nanophotocatalysts have numerous applications in the field of water splitting, dissociation of volatile organic pollutants, organic synthesis, degradation of dyes/hazardous contaminants, cancer cells inactivation, self-cleaning surfaces, hydrogen evolution, photo-electrochemical conversion, etc. Typically, to produce nanophotocatalysts, diverse conventional physicochemical strategies have been reported with some important drawbacks/limitations such as the utilization of toxic/hazardous materials, complex/expensive instruments, and time-consuming reactions. Therefore, there is a high demand for developing green, environmentally friendly, and cost-effective synthetic tactics, which can reduce or eliminate the rigorousness and complications of the conventional approaches. These nanophotocatalysts have shown high stability, good recyclability, and remarkable catalytic activity. Typically, the significant specific surface areas, the abundant functional groups, large amounts of active sites are the important advantages of the nanoscaled structures for highly photocatalytic degradation of organic pollutants. However, more elaborative studies are still needed to overcome some important limitations/drawbacks of nanophotocatalysts for industrial applications, which include the difficult separation, low selectivity, aggregation/sedimentation, low-usage of visible light, fast charge recombination, and low migration potential of photo-generated electrons and holes. This review highlights recent advances related to the greener and eco-friendly synthesis of nanophotocatalysts, as well as their environmental photocatalytic applications. Graphical Abstract","PeriodicalId":10481,"journal":{"name":"Comments on Inorganic Chemistry","volume":"48 1","pages":"133 - 187"},"PeriodicalIF":5.4,"publicationDate":"2021-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89081474","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-01-31DOI: 10.1080/02603594.2020.1870963
Reem G. Deghadi, Ayman S. Eliwa, Aya E. Ali, W. Hosny, G. Mohamed
ABSTRACT A new organic linker Schiff base (H2L) derived from 4-aminobenzoic acid and 2-carboxybenzaldehyde has been successfully synthesized and characterized. The synthesized linker Schiff base was designed to be used in preparation of a new cadmium-based metal-organic framework (Cd-MOF) by sonochemical synthesis, and characterized by using Fourier-transform infrared spectroscopy (FT-IR), powder X-ray diffraction (PXRD), Brunauer-Emmett-Teller (BET), scanning electron microscope (SEM), energy dispersive X-ray (EDX), and thermal analysis. Under an optimum set of synthesis conditions, uniform cubic crystals with average size 44–69 nm and a Langmuir surface area of 163.461 m2/g were produced within 60–75 min by crystal system orthorhombic. The synthesized Cd-MOF was incorporated as an ionophore in a carbon paste electrode for Cu(II) ion determination in different real water samples. The proposed carbon paste electrode showed a Nernstian slope of 30.15 ± 0.35 mV decade−1 covering a linear range of 1.0 × 10−7 – 1.0 × 10−1 mol L−1 and the detection limit was 7.5 × 10−8 mol L−1 with long-time stability of more than two months over pH range of 2.5–6.5 and fast response time of 10 s. The proposed sensor was highly selective for Cu(II) ions. The synthesized Cd-MOF had mesoporous structure and this supported the mechanism of Cu(II) ion successful determination.
{"title":"Preparation, Characterization of Novel Cadmium-Based Metal-Organic Framework for Using as a Highly Selective and Sensitive Modified Carbon Paste Electrode in Determination of Cu(II) Ion","authors":"Reem G. Deghadi, Ayman S. Eliwa, Aya E. Ali, W. Hosny, G. Mohamed","doi":"10.1080/02603594.2020.1870963","DOIUrl":"https://doi.org/10.1080/02603594.2020.1870963","url":null,"abstract":"ABSTRACT A new organic linker Schiff base (H2L) derived from 4-aminobenzoic acid and 2-carboxybenzaldehyde has been successfully synthesized and characterized. The synthesized linker Schiff base was designed to be used in preparation of a new cadmium-based metal-organic framework (Cd-MOF) by sonochemical synthesis, and characterized by using Fourier-transform infrared spectroscopy (FT-IR), powder X-ray diffraction (PXRD), Brunauer-Emmett-Teller (BET), scanning electron microscope (SEM), energy dispersive X-ray (EDX), and thermal analysis. Under an optimum set of synthesis conditions, uniform cubic crystals with average size 44–69 nm and a Langmuir surface area of 163.461 m2/g were produced within 60–75 min by crystal system orthorhombic. The synthesized Cd-MOF was incorporated as an ionophore in a carbon paste electrode for Cu(II) ion determination in different real water samples. The proposed carbon paste electrode showed a Nernstian slope of 30.15 ± 0.35 mV decade−1 covering a linear range of 1.0 × 10−7 – 1.0 × 10−1 mol L−1 and the detection limit was 7.5 × 10−8 mol L−1 with long-time stability of more than two months over pH range of 2.5–6.5 and fast response time of 10 s. The proposed sensor was highly selective for Cu(II) ions. The synthesized Cd-MOF had mesoporous structure and this supported the mechanism of Cu(II) ion successful determination.","PeriodicalId":10481,"journal":{"name":"Comments on Inorganic Chemistry","volume":"23 1","pages":"189 - 212"},"PeriodicalIF":5.4,"publicationDate":"2021-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77254905","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
ABSTRACT Luminescent metal-organic frameworks (LMOFs), as a subclass of MOFs, have attracted great attention, due to their promising potentials in practical applications. Therefore, as chemosensors, by combining the characteristic luminescent properties and the diversiform topological structures, LMOFs open up promising potentials for sensing. Nitroaromatic compounds (NACs) pose a great threat for environment and homeland security because of their toxicity and explosiveness, and then developing sensitive, selective, and reversible sensors for NACs is in great demand. In this review, we summarize recent works on LMOFs sensors for NACs through photophysical properties, sensing behaviors, possible mechanisms, existing problems and prospects for further developments. Graphical Abstract
{"title":"Luminescent Metal-Organic Frameworks for Nitroaromatic Compounds Detection","authors":"Tianhao Zhao, Fenhang Zhang, Jing Zhou, Xiaoqing Zhao","doi":"10.1080/02603594.2020.1853537","DOIUrl":"https://doi.org/10.1080/02603594.2020.1853537","url":null,"abstract":"ABSTRACT Luminescent metal-organic frameworks (LMOFs), as a subclass of MOFs, have attracted great attention, due to their promising potentials in practical applications. Therefore, as chemosensors, by combining the characteristic luminescent properties and the diversiform topological structures, LMOFs open up promising potentials for sensing. Nitroaromatic compounds (NACs) pose a great threat for environment and homeland security because of their toxicity and explosiveness, and then developing sensitive, selective, and reversible sensors for NACs is in great demand. In this review, we summarize recent works on LMOFs sensors for NACs through photophysical properties, sensing behaviors, possible mechanisms, existing problems and prospects for further developments. Graphical Abstract","PeriodicalId":10481,"journal":{"name":"Comments on Inorganic Chemistry","volume":"22 1","pages":"100 - 132"},"PeriodicalIF":5.4,"publicationDate":"2020-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85824812","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-10-29DOI: 10.1080/02603594.2020.1837783
Mutasem Z. Bani-Fwaz
ABSTRACT This review article focuses on 1λ3-phosphaalkene compounds derived from phosphines containing at least one silicon-phosphorous bond. 1λ3-Phosphaalkene compounds are of high value as they are used to form several phosphorous compounds containing a transition metal and main group elements. In addition to the fact that different kinds of 1λ3-phosphaalkynes are prepared from 1λ3-phosphaalkenes. Both families of phosphorous compounds; 1λ3-phosphaalkenes and 1λ3-phosphaalkynes have become important to chemists, as they are used in preparing several phosphorous compounds to be used as homogeneous catalysts in chemical reactions. GRAPHICAL ABSTRACT
{"title":"Main Group and Transition Metal-Mediated Phosphaalkene Insertion Reactions Initiated by Phosphines Containing Si–P Bond","authors":"Mutasem Z. Bani-Fwaz","doi":"10.1080/02603594.2020.1837783","DOIUrl":"https://doi.org/10.1080/02603594.2020.1837783","url":null,"abstract":"ABSTRACT This review article focuses on 1λ3-phosphaalkene compounds derived from phosphines containing at least one silicon-phosphorous bond. 1λ3-Phosphaalkene compounds are of high value as they are used to form several phosphorous compounds containing a transition metal and main group elements. In addition to the fact that different kinds of 1λ3-phosphaalkynes are prepared from 1λ3-phosphaalkenes. Both families of phosphorous compounds; 1λ3-phosphaalkenes and 1λ3-phosphaalkynes have become important to chemists, as they are used in preparing several phosphorous compounds to be used as homogeneous catalysts in chemical reactions. GRAPHICAL ABSTRACT","PeriodicalId":10481,"journal":{"name":"Comments on Inorganic Chemistry","volume":"41 1","pages":"67 - 99"},"PeriodicalIF":5.4,"publicationDate":"2020-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80066805","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-09-29DOI: 10.1080/02603594.2020.1821674
Ahmad Jonidi Jafari, Mehrdad Moslemzadeh
ABSTRACT Objective is to investigate effect of preparation methods on crystal size at synthesis of Fe-doped TiO2 as a systematic review study. All references (455) were found by manual duplication and finally n = 136 records remained. After reading their titles, abstracts and full-texts, 58 relevant full-text articles were included based on the considered exclusion criteria. Finally, 21 relevant full-text articles, which consisted of crystal size data, were selected to conduct this systematic review study. The relevant publications were from 2005 to 2019. In 14 studies (66.67%), Fe-doped TiO2 was prepared by sol-gel method. In many of the studies related to sol-gel method, crystal sizes range from 5 to 25 nm. Among the applied methods for preparation of Fe-doped TiO2, ultrasonic and microwave methods on crystal sizes 58 nm and 170.24 nm were the highest volume. In general, even though the studies used the same procedures, they reported different results. It is concluded that in these studies, in addition to preparation methods, other parameters could be effected on the crystal sizes, such as type of Ti procurers. However, that should be investigated in future studies as a systematic review.
{"title":"Synthesis of Fe-Doped TiO2 for Photocatalytic Processes under UV-Visible Light: Effect of Preparation Methods on Crystal Size—A Systematic Review Study","authors":"Ahmad Jonidi Jafari, Mehrdad Moslemzadeh","doi":"10.1080/02603594.2020.1821674","DOIUrl":"https://doi.org/10.1080/02603594.2020.1821674","url":null,"abstract":"ABSTRACT Objective is to investigate effect of preparation methods on crystal size at synthesis of Fe-doped TiO2 as a systematic review study. All references (455) were found by manual duplication and finally n = 136 records remained. After reading their titles, abstracts and full-texts, 58 relevant full-text articles were included based on the considered exclusion criteria. Finally, 21 relevant full-text articles, which consisted of crystal size data, were selected to conduct this systematic review study. The relevant publications were from 2005 to 2019. In 14 studies (66.67%), Fe-doped TiO2 was prepared by sol-gel method. In many of the studies related to sol-gel method, crystal sizes range from 5 to 25 nm. Among the applied methods for preparation of Fe-doped TiO2, ultrasonic and microwave methods on crystal sizes 58 nm and 170.24 nm were the highest volume. In general, even though the studies used the same procedures, they reported different results. It is concluded that in these studies, in addition to preparation methods, other parameters could be effected on the crystal sizes, such as type of Ti procurers. However, that should be investigated in future studies as a systematic review.","PeriodicalId":10481,"journal":{"name":"Comments on Inorganic Chemistry","volume":"1 1","pages":"327 - 346"},"PeriodicalIF":5.4,"publicationDate":"2020-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79995065","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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